Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 780184015 | Factor V deficiency (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
| 8280018 | Factor V deficiency | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 8281019 | Factor V deficiency, NOS | en | Synonym | Inactive | Initial character case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Factor V deficiency | Interprets | Haemostatic function | true | Inferred relationship | Some | 1 | |
| Factor V deficiency | Has interpretation | Abnormal | true | Inferred relationship | Some | 1 | |
| Factor V deficiency | Is a | Coagulation factor deficiency syndrome | true | Inferred relationship | Some | ||
| Factor V deficiency | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Factor V deficiency | Has definitional manifestation | Haemostatic system finding | false | Inferred relationship | Some | ||
| Factor V deficiency | Finding site | Entire haematological system | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Acquired factor V deficiency disease | Is a | True | Factor V deficiency | Inferred relationship | Some | |
| Hereditary factor V deficiency disease | Is a | True | Factor V deficiency | Inferred relationship | Some | |
| Combined deficiency of factor V and factor VIII | Is a | True | Factor V deficiency | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Australian dialect reference set
Problem/Diagnosis reference set
FHIR